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Experimental Neurology|January 4, 2011
Longitudinal behavioral, cross-sectional transcriptional and histopathological characterization of a knock-in mouse model of Huntington's disease with 140 CAG repeatsAaron C Rising, Jia Xu, Aaron Carlson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 27, 2009
Tight Long-term dynamic doxycycline responsive nigrostriatal GDNF using a single rAAV vectorFredric P Manfredsson, Corinna Burger, Aaron C Rising, et al.
Human Molecular Genetics|April 26, 2011
Transgenic mice expressing caspase-6-derived N-terminal fragments of mutant huntingtin develop neurologic abnormalities with predominant cytoplasmic inclusion pathology composed largely of a smaller proteolytic derivativeAndrew T N Tebbenkamp, Cameron Green, Guilian Xu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2009
Nigrostriatal rAAV-mediated GDNF overexpression induces robust weight loss in a rat model of age-related obesityFredric P Manfredsson, Nihal Tumer, Benedek Erdos, et al.
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